CC BY-NC-ND 4.0 · Endoscopy 2022; 54(S 02): E1072-E1073
DOI: 10.1055/a-1918-1639
E-Videos

Complete resection of residual rectal dysplasia in a patient with ulcerative colitis using the pocket-creation method

Toshihiro Fujinuma
1   Department of Medicine, Division of Gastroenterology, Jichi Medical University, Shimotsuke, Japan
,
Takahito Takezawa
1   Department of Medicine, Division of Gastroenterology, Jichi Medical University, Shimotsuke, Japan
,
Masahiro Okada
1   Department of Medicine, Division of Gastroenterology, Jichi Medical University, Shimotsuke, Japan
,
1   Department of Medicine, Division of Gastroenterology, Jichi Medical University, Shimotsuke, Japan
,
Yusuke Amano
2   Department of Integrative Pathology, Jichi Medical University, Shimotsuke, Japan
,
3   Department of Surgery, Jichi Medical University, Shimotsuke, Japan
,
1   Department of Medicine, Division of Gastroenterology, Jichi Medical University, Shimotsuke, Japan
› Author Affiliations
 

Formerly, when ulcerative colitis-associated neoplasia (UCAN) was identified, total colectomy was required to prevent future colorectal cancers. Since the introduction of the SCENIC guideline (2015) [1], endoscopic resection of UCAN is gradually being accepted. UCANs are however obscurely demarcated and have severe submucosal fibrosis, which makes endoscopic R0 resection challenging. Although multiple biopsies can be helpful to demarcate UCAN, they make the resection more challenging. The pocket-creation method (PCM) of endoscopic submucosal dissection (ESD) is good for resecting fibrotic submucosa, such as that under nongranular laterally spreading tumors [2] or after endoscopic interventions including biopsies. We illustrate the complete endoscopic resection of an area of rectal dysplasia in a patient with UC using the PCM.

The patient was a 67-year-old man who had an 18-year history of UC. Although he had undergone endoscopic mucosal resection (EMR) of an adenoma in the distal rectum 3 years previously, the resection margin was pathologically positive, and a surveillance colonoscopy 2 years after the resection revealed residual dysplasia. He was referred to our hospital because he wanted to undergo endoscopic local resection instead of total colectomy. After he had received 3 months of concurrent treatment with 5-aminosalicylic acid enemas for the still inflamed rectum, along with oral 5-aminosalicylic acid and vedolizumab, a slightly red elevated lesion was identified ([Fig. 1]). Multiple biopsies were taken from this elevated area and also from the surrounding mucosa to determine the extent of the dysplasia, with the outermost biopsies being found to be negative for dysplasia.

Zoom Image
Fig. 1 Endoscopic images showing the elevated rectal lesion: a on magnifying colonoscopy (EC-760ZP-W/M, Fujifilm, Tokyo, Japan), which revealed a 10-mm red slightly elevated lesion close to the dentate line (“X” indicates a biopsy that was pathologically positive for dysplasia; “O” indicates a biopsy that was pathologically negative for dysplasia); b following indigo carmine spraying, which enhanced the area surrounding the lesion (red dotted line indicates the area identified as dysplasia on biopsy results).

The PCM was performed after the area of dysplasia had been demarcated by reference to the surrounding negative biopsies ([Video 1]). Despite severe submucosal fibrosis caused by chronic inflammation, the previous EMR, and the multiple biopsies ([Fig. 2]), en bloc resection was achieved, without any adverse events. Pathologic evaluation revealed a low grade dysplastic lesion, with a negative margin ([Fig. 3]).

Video 1 Complete resection of residual rectal dysplasia after endoscopic mucosal resection in a patient with ulcerative colitis using the pocket-creation method of endoscopic submucosal dissection.


Quality:
Zoom Image
Fig. 2 Images during performance of the pocket-creation method of endoscopic submucosal dissection using a therapeutic gastroscope (EG-L580RD, Fujifilm), 1.5-mm ORISE Proknife (Boston Scientific, Marlborough, Massachusetts, USA), ST hood (DH-33GR, Fujifilm), and VIO 3 (ERBE Elektromedizin, Tübingen, Germany) showing: a severe focal submucosal fibrosis on entering the submucosal pocket, which was likely caused by the endoscopic mucosal resection 3 years previously; b fibrosis of the entire submucosa due to chronic inflammation from ulcerative colitis and the previous multiple biopsies.
Zoom Image
Fig. 3 Macroscopic appearance of the resected specimen after formalin fixation (the left side is distal), which was shown to be low grade dysplasia with a negative margin (blue lines indicate the dysplasia). All pathological specimens showed negative p53 immunostaining, consistent with this being sporadic dysplasia or ulcerative colitis-associated neoplasia with null mutant of the p53 gene.

This patient demonstrates that rectal dysplasia with severe submucosal fibrosis due to UC and previous multiple endoscopic interventions can be safely and completely resected using the PCM.

Endoscopy_UCTN_Code_CCL_1AD_2AD

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Competing interests

H. Yamamoto is a consultant for Fujifilm Corporation and has received honoraria, a grant and royalties from the company. The remaining authors declare that they have no conflict of interest.

  • References

  • 1 Laine L, Kaltenbach T, Barkun A. et al. SCENIC international consensus statement on surveillance and management of dysplasia in inflammatory bowel disease. Gastroenterology 2015; 148: 639-651 e628
  • 2 Sakamoto H, Hayashi Y, Miura Y. et al. Pocket-creation method facilitates endoscopic submucosal dissection of colorectal laterally spreading tumors, non-granular type. Endosc Int Open 2017; 5: E123-E129

Corresponding author

Yoshikazu Hayashi, MD, PhD
Department of Medicine, Division of Gastroenterology
Jichi Medical University
3311-1 Yakushiji, Shimotsuke
Tochigi
Japan   

Publication History

Article published online:
01 September 2022

© 2022. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

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  • References

  • 1 Laine L, Kaltenbach T, Barkun A. et al. SCENIC international consensus statement on surveillance and management of dysplasia in inflammatory bowel disease. Gastroenterology 2015; 148: 639-651 e628
  • 2 Sakamoto H, Hayashi Y, Miura Y. et al. Pocket-creation method facilitates endoscopic submucosal dissection of colorectal laterally spreading tumors, non-granular type. Endosc Int Open 2017; 5: E123-E129

Zoom Image
Fig. 1 Endoscopic images showing the elevated rectal lesion: a on magnifying colonoscopy (EC-760ZP-W/M, Fujifilm, Tokyo, Japan), which revealed a 10-mm red slightly elevated lesion close to the dentate line (“X” indicates a biopsy that was pathologically positive for dysplasia; “O” indicates a biopsy that was pathologically negative for dysplasia); b following indigo carmine spraying, which enhanced the area surrounding the lesion (red dotted line indicates the area identified as dysplasia on biopsy results).
Zoom Image
Fig. 2 Images during performance of the pocket-creation method of endoscopic submucosal dissection using a therapeutic gastroscope (EG-L580RD, Fujifilm), 1.5-mm ORISE Proknife (Boston Scientific, Marlborough, Massachusetts, USA), ST hood (DH-33GR, Fujifilm), and VIO 3 (ERBE Elektromedizin, Tübingen, Germany) showing: a severe focal submucosal fibrosis on entering the submucosal pocket, which was likely caused by the endoscopic mucosal resection 3 years previously; b fibrosis of the entire submucosa due to chronic inflammation from ulcerative colitis and the previous multiple biopsies.
Zoom Image
Fig. 3 Macroscopic appearance of the resected specimen after formalin fixation (the left side is distal), which was shown to be low grade dysplasia with a negative margin (blue lines indicate the dysplasia). All pathological specimens showed negative p53 immunostaining, consistent with this being sporadic dysplasia or ulcerative colitis-associated neoplasia with null mutant of the p53 gene.